Kanai Y, Hori S, Tanaka T, Yasuoka M, Watanabe K, Aikawa N, Hosoda Y
Keio University School of Medicine, Tokyo, Japan.
Cardiovasc Res. 1993 Sep;27(9):1619-23. doi: 10.1093/cvr/27.9.1619.
The aim was to clarify the role of serotonin (5-hydroxytryptamine, 5-HT) in monocrotaline induced pulmonary hypertension.
Plasma 5-HT levels, pulmonary capillary platelet count, and vascular responsiveness to 5-HT were evaluated in the model. The effects of the selective 5-HT2 receptor antagonist, DV-7028, on the development of pulmonary hypertension were also investigated.
Plasma 5-HT was raised 12 h to 3 d after monocrotaline administration (60 mg.kg-1), coinciding with accumulation of platelets in the pulmonary circulation. Isolated pulmonary arteries showed hyperreactivity to 5-HT at 14 and 21 d after monocrotaline. Administration of DV-7028 (20 mg.kg-1 x d-1) attenuated the increase in pulmonary arterial pressure, right ventricular hypertrophy, and medial thickening of the pulmonary arteries.
The present study suggests that 5-HT released from platelets contributes to the initiation and progression of monocrotaline induced pulmonary hypertension.
旨在阐明血清素(5-羟色胺,5-HT)在野百合碱诱导的肺动脉高压中的作用。
在该模型中评估血浆5-HT水平、肺毛细血管血小板计数以及血管对5-HT的反应性。还研究了选择性5-HT2受体拮抗剂DV-7028对肺动脉高压发展的影响。
给予野百合碱(60mg·kg-1)后12小时至3天,血浆5-HT升高,这与血小板在肺循环中的积聚相一致。野百合碱给药后14天和21天,离体肺动脉对5-HT表现出高反应性。给予DV-7028(20mg·kg-1×d-1)可减轻肺动脉压升高、右心室肥厚以及肺动脉中膜增厚。
本研究表明,血小板释放的5-HT有助于野百合碱诱导的肺动脉高压的起始和进展。